Medical Device Manufacturer · US , Mchenry , IL

Poirier S.A. - FDA 510(k) Cleared Devices

17 submissions · 17 cleared · Since 1984
17
Total
17
Cleared
0
Denied

Poirier S.A. has 17 FDA 510(k) cleared physical medicine devices. Based in Mchenry, US.

Historical record: 17 cleared submissions from 1984 to 1984.

Browse the complete list of FDA 510(k) cleared physical medicine devices from this manufacturer. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Poirier S.A.

17 devices
1-12 of 17
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